| Tag | Content |
|---|
EnhancerAtlas ID | HS050-01767 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:38096380-38097240 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr1:38096924-38096934 | CTCAAGTGGT | - | 6.02 | | RREB1 | MA0073.1 | chr1:38096495-38096515 | ACCCCACACTCCCCCACACA | + | 6.09 | | RREB1 | MA0073.1 | chr1:38096505-38096525 | CCCCCACACACACCCACACC | + | 7.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGACATCTGA GCCCAACCTG GGAGTGAGAA TGAAAACCCT GCTTCCCCGT CACGGGATCA 60
CACACATGCT CTGATGCTCT CAAGGTTCTT CCACAGCAGC GGCCTGCCCA CGCACACCCC 120
ACACTCCCCC ACACACACCC ACACCACAAC AGAGCATGCA GGCCAATAGC ACAGAGTCTC 180
TGTAGATGCC AGGGAGCCAT CACCTTCCCC TCCAGTGGCT AGATGCCTTC GAACAAGTCA 240
TGTAGCCTCA CTGAACCTGT TTCACATCTA TAAAATGGGG ACAAGCATGA CTATGTCACA 300
GGCTAGCTGA GAGTCAGAGA GTTCAGGCTC AGGAATGAGA AATCTGAGGT GCTGGAGTGG 360
AGGTGCCCCT CCCACCCCCT GTCCTAATCC TTTCCCCTCT AGGCTCTTCA GTGCCAGTCC 420
ACCCCCTCGC CTGTCAGGGA GGCCCCAGCA GAGCCCACCT GCACGGGAGA TAAATCATTA 480
TCCCCTAAGG GAGTTCAGTA CCTCCCTCCT TGGCCTCTCC CGCTGGCTTT GAAGGCCAGA 540
CACACTCAAG TGGTTAAGCT GCCTGTGAGA AGTGTTTACA TGAGGCTGAT GGATCCCACC 600
TGGTGCTGTG GCCTGAGCCA GAGGAGATGC CCCCAGCTAC CCCCAAATGC CCGTCAGCTG 660
CCAACCCCTG CACGCCCCTC CAGTACTCCC TGCCTGATTT ACCAAAGCCT TTCTATCCTC 720
CCCAGCCCCC ACTACACAAT TCTCTCACCC ACAGATTATA GATGTCCAGT TGAGTTTATC 780
AAACTGGGGT CTTCTGGCCC AAGTCTGTAG TCTCAGAGGC TGGCTGTACA GCATGATAGT 840
CACGGGCATA AACTTCAGAG 860
|
